Informations:
Erreur:
ID
32628
Description
Cotransplantation of Islet and Mesenchymal Stem Cell in Type 1 Diabetic Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00646724
Lien
https://clinicaltrials.gov/show/NCT00646724
Mots-clés
Versions (1)
- 08/11/2018 08/11/2018 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
8 novembre 2018
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
Modèle Commentaires :
Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.
Groupe Item commentaires pour :
Item commentaires pour :
Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.
Eligibility Type 1 Diabetes Mellitus NCT00646724
Eligibility Type 1 Diabetes Mellitus NCT00646724
- StudyEvent: Eligibility
Similar models
Eligibility Type 1 Diabetes Mellitus NCT00646724
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Age
Item
male and female patients age 18 to 60 years of age
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
ability to provide written informed consent
boolean
C0021430 (UMLS CUI [1])
Signs and Symptoms Severe | Disability
Item
manifest signs and symptoms that are severe enough to be incapacitating
boolean
C0037088 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0231170 (UMLS CUI [2])
C0205082 (UMLS CUI [1,2])
C0231170 (UMLS CUI [2])
Diabetes mellitus poor control | Hemoglobin A1c measurement
Item
patients with poor diabetes control (hba1c > 7% but < 12%)
boolean
C0860161 (UMLS CUI [1])
C0474680 (UMLS CUI [2])
C0474680 (UMLS CUI [2])
Complications of Diabetes Mellitus Progressive
Item
progressive diabetic complications
boolean
C0342257 (UMLS CUI [1,1])
C0205329 (UMLS CUI [1,2])
C0205329 (UMLS CUI [1,2])
Age
Item
age < 18 years or > 60 years
boolean
C0001779 (UMLS CUI [1])
Diabetes Mellitus Disease length
Item
diabetic history < 5 years
boolean
C0011849 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
C0872146 (UMLS CUI [1,2])
Body mass index
Item
bmi > 27
boolean
C1305855 (UMLS CUI [1])
Body Weight
Item
body weight > 80 kg
boolean
C0005910 (UMLS CUI [1])
Requirement Insulin Exogenous U/kg/day
Item
exogenous insulin requirement > 1 unit/kg/day
boolean
C1514873 (UMLS CUI [1,1])
C0021641 (UMLS CUI [1,2])
C0205228 (UMLS CUI [1,3])
C1532634 (UMLS CUI [1,4])
C0021641 (UMLS CUI [1,2])
C0205228 (UMLS CUI [1,3])
C1532634 (UMLS CUI [1,4])
Anemia, severe | Gender
Item
severe anemia (male < 8 g/dl, female < 7 g/dl)
boolean
C0238644 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
C0079399 (UMLS CUI [2])
White blood cell count decreased
Item
low white blood cell count (< 3000/dl)
boolean
C0750394 (UMLS CUI [1])
Liver Dysfunction
Item
liver dysfunction
boolean
C0086565 (UMLS CUI [1])
Communicable Disease | Hepatitis B | Hepatitis C | HIV Infection | Tuberculosis
Item
active infection including hepatitis b, hepatitis c, hiv, or tb
boolean
C0009450 (UMLS CUI [1])
C0019163 (UMLS CUI [2])
C0019196 (UMLS CUI [3])
C0019693 (UMLS CUI [4])
C0041296 (UMLS CUI [5])
C0019163 (UMLS CUI [2])
C0019196 (UMLS CUI [3])
C0019693 (UMLS CUI [4])
C0041296 (UMLS CUI [5])
Panel-reactive antibody
Item
panel reactive antibody > 20%
boolean
C1141951 (UMLS CUI [1])
Medical condition Interferes with Completion of clinical trial
Item
any medical condition that, in the opinion of the investigator, will interfere with the safe completion of the trial
boolean
C3843040 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C2732579 (UMLS CUI [1,3])
C0521102 (UMLS CUI [1,2])
C2732579 (UMLS CUI [1,3])